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Adolescent Idiopathic Scoliosis clinical trials

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NCT ID: NCT01661959 Enrolling by invitation - Clinical trials for Adolescent Idiopathic Scoliosis

Adolescent Idiopathic Scoliosis Outcomes Database Registry

AIS
Start date: January 2005
Phase:
Study type: Observational

The purpose of this study is to analyze the long-term outcomes of surgical treatment of idiopathic scoliosis of all curve patterns treated by either anterior or posterior procedures. In addition, to analyze the long-term outcomes of non-operative idiopathic scoliosis.

NCT ID: NCT01633931 Active, not recruiting - Clinical trials for Adolescent Idiopathic Scoliosis

Treatment of Adolescent Idiopathic Scoliosis Patients Using the Ellipse MAGEC System

Start date: March 2012
Phase: N/A
Study type: Observational

The purpose of this study is to collect data on the use of the Ellipse MAGEC System to treat patients with adolescent idiopathic scoliosis (AIS) who have failed external brace therapy.

NCT ID: NCT01581021 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Pedicle Screw Usage in Conventional Fixation Pattern Constructs Compared to Thoracic Hook Constructs in Scoliosis

Start date: August 2005
Phase: N/A
Study type: Interventional

Scoliosis is a deformity in which there is an abnormal curvature of the spine. Surgery is the main method of correcting this deformity. Rods are attached to the spine to make it strait. There are two ways to fix these rods to the bone of the spine: laminar hooks or pedicle screws. Hooks are an older form of fixation and do not penetrate the bone, but are instead placed over a part of the vertebra called the lamina. Screws are newer and do penetrate the bone. Screws are placed into the part of the vertebra called the pedicle. Most surgeons think screws correct scoliosis better than hooks. The current literature agrees that screws are better for deformity correction in the lumbar spine and patients with severe deformity. There is disagreement in the literature regarding which works better in the thoracic spine in less severe deformity. There are no randomized, controlled trials in the literature that examine whether constructs that use hooks in the thoracic spine and screws in the lumbar spine (called hybrid constructs) work as well as all-screw constructs. This clinical study is a randomized controlled trial being conducted to evaluate treatment outcomes in patients with scoliosis undergoing surgical correction for their curves using either all-screw or hybrid constructs as fixation devices. The study population is limited to those with less severe deformity and the investigators' hypothesis is that hybrid constructs will be as acceptable as screws in terms of correction.

NCT ID: NCT01550497 Completed - Low Back Pain Clinical Trials

Spinal Stabilization Exercises for Low Back Pain in Adolescents With Idiopathic Scoliosis

LBPAIS
Start date: March 1, 2012
Phase: N/A
Study type: Interventional

1. Do spinal stabilization exercises demonstrate immediate and long-term effects of weight weeks of spinal stabilization exercises as measured by pain intensity and quality of life scores? 2. Does eight weeks of spinal stabilization exercises improve back muscle endurance in adolescents with Idiopathic Scoliosis (IS) with low back pain (LBP), compared to a one-time treatment (control)? Hypotheses: The research hypothesis for Question 1 is: Participants who receive eight weeks of spinal stabilization exercises will demonstrate significantly improved pain intensity and quality of life scores compared to participants who receive a one-time treatment after eight weeks of the intervention period and at six-month follow-up. The research hypothesis for Question 2 is: Participants who receive eight weeks of the spinal stabilization exercises will demonstrate significantly improved back muscle endurance, compared to participants who receive a one-time treatment after eight weeks of intervention.

NCT ID: NCT01451788 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Effect of Human Thrombin With Gelatin Matrix on Perioperative Blood Loss in Scoliosis Surgery

Start date: November 2011
Phase: Phase 4
Study type: Interventional

The Finnish Paediatric Orthopaedic Study Group will perform a prospective randomized, multicenter, clinical trial comparing Gelatin matrix with human derived thrombin (Floseal, Baxter) and without use of Floseal in adolescents undergoing posterior spinal deformity surgery for AIS (adolescent idiopathic scoliosis between 45 and 90 degrees) in Turku, Tampare and Helsinki Children's Hospitals. Sixty patients will be randomized into the intervention group receiving Floseal (n=30) and control group not receiving Floseal (n=30). Each University Hospital will treat 10 Floseal and 10 conventional treated scoliosis patients (block randomization). Both treatment groups will be allowed to use conventional blood saving methods.

NCT ID: NCT00989495 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

Comprehensive Cohort Study of Bracing for Adolescent Idiopathic Scoliosis (AIS): A Feasibility Study

Start date: October 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to gain initial experience and information for proper planning and conduct of a confirmatory study (a multi-centre single-blind comprehensive cohort study of bracing).

NCT ID: NCT00958373 Withdrawn - Clinical trials for Adolescent Idiopathic Scoliosis

Risk Factors for Psychiatric Disorders Associated With Adolescent Idiopathic Scoliosis

Start date: October 2006
Phase: N/A
Study type: Observational

The purpose of this pilot study is to determine the presence, frequency, and severity of mental health disorders amongst adolescents undergoing spinal surgery for scoliosis.

NCT ID: NCT00886652 Completed - Clinical trials for Adolescent Idiopathic Scoliosis

An Aerobic Exercising Program on Respiratory Muscle Strength in Patients With Adolescent Idiopathic Scoliosis

Start date: January 2008
Phase: N/A
Study type: Interventional

Adolescent Idiopathic Scoliosis (AIS) can change the respiratory dynamics and performance of the inspiratory and expiratory muscles, affecting ventilatory capacity. This was a randomized, controlled, open study to test the impact of a physiotherapeutic program of aerobic exercises on respiratory muscle strength, in patients with adolescent idiopathic scoliosis. Patients with AIS were randomly assigned to the aerobic exercise-training program group or the no treatment group. There was a significant increase in Pimax and Pemax in the group which received physiotherapy.

NCT ID: NCT00448448 Terminated - Clinical trials for Adolescent Idiopathic Scoliosis

Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST)

BrAIST
Start date: February 2007
Phase: N/A
Study type: Interventional

Adolescent idiopathic scoliosis (AIS) is a structural curve of the spine with no clear underlying cause. Bracing is currently the standard of care for preventing curve progression and treating AIS. However, the effectiveness of bracing remains unclear. The purpose of this study is to compare the risk of curve progression in adolescents with AIS who wear a brace versus those who do not and to determine whether there are reliable factors that can predict the usefulness of bracing for a particular individual with AIS.